Sponsor‑Dedicated Clinical Research Associate (CRA)

IQVIA; Littleton (CO); Sur place; USD 75 000 - 198 000; Plein temps

Résumé du poste

IQVIA is seeking a Clinical Research Associate to perform site monitoring visits and ensure protocol adherence across studies in the United States. You will train site personnel, manage regulatory submissions, and oversee data quality with the study team.

Minimum 2 years of on-site CRA experience and a Bachelor’s degree are required; strong communication and organizational skills are essential.

Qualifications

• Bachelor's degree in scientific discipline or health care preferred.
• Requires at least 2 years of on-site CRA experience in a CRO, sponsor, or similar setting.
• Good knowledge of GCP and ICH guidelines.
• Proficient in Word, Excel, PowerPoint; familiarity with trial systems.

Responsabilités

• Perform site monitoring visits (selection, initiation, monitoring and close-out) per scope of work and GCP.
• Drive subject recruitment plans with sites to improve predictability.
• Administer protocol training and maintain regular communication with sites.

Connaissances

On-site monitoring

English communication

Project coordination

Regulatory knowledge

Formation

Bachelor's degree in scientific discipline or health care

Outils

EDC

CTMS

eTMF

IVRS/IWRS

Description du poste

IQVIA is seeking a Clinical Research Associate to perform site monitoring visits and ensure protocol adherence across studies in the United States. You will train site personnel, manage regulatory submissions, and oversee data quality with the study team.

Minimum 2 years of on-site CRA experience and a Bachelor’s degree are required; strong communication and organizational skills are essential.